Lithium-aluminosilicate glass ceramic with high keatite content and structural member made thereof

ABSTRACT

A lithium-aluminosilicate glass ceramic is transformed by a suitable heat treatment into a glass ceramic comprising at least 80 vol.-% of keatite mixed crystals. This may be utilized for the preparation of optical or mechanical high-precision parts having a high temperature resistance, a good stability and compatibility with components consisting of metals having a small coefficient of thermal expansion based on nickel and iron, such as Invar®.

CROSS-REFERENCE TO RELATED APPLICATIONS

This present application is a divisional of U.S. application Ser. No.10/638,823, filed Aug. 11, 2003 now U.S. Pat. No. 7,107,793, whichclaims priority of German Patent Application No. 102 38 608.0, filedAug. 16, 2002.

BACKGROUND OF THE INVENTION

The invention relates to a lithium-aluminosilicate glass ceramic of aparticular kind and to a method for preparing such a glass ceramic.

The invention further relates to a composite component comprising atleast a first component of a lithium-aluminosilicate glass ceramic andat least a second component of a metal alloy having a low coefficient ofthermal expansion.

The invention further relates to novel utilizations of alithium-aluminosilicate glass ceramic.

Since years the applicant has successfully used Zerodur® glass ceramicsas precision parts for optical and mechanical applications. The glassceramic Zerodur® is a lithium-aluminosilicate glass ceramic that isprepared from a base glass of the system Li₂O—Al₂O₃—SiO₂, wherein by theaddition of nucleation agents such as TiO₂ or ZrO₂ a controlledcrystallization is effected (confer German examined application DE1,902,432). In addition, from U.S. Pat. No. 4,851,372 a similar glassceramic has become known which is marketed by the applicant under themark Zerodur-M®.

These glass ceramics are prepared in several steps. After melting andhot forming usually the base glass is cooled to a temperature below theglass transition temperature. Thereafter the base glass is transformedinto a glass ceramic article by controlled crystallization. Thisceramization is performed by an annealing process having several stepsin which in the beginning nuclei are formed by nucleation at atemperature between 600 and 800° C., usually from TiO₂ or ZrO₂/TiO₂mixed crystals. Also SnO₂ may take part in the nucleation. During asubsequent raise of temperature high quartz mixed crystals grow on thesenuclei at a crystallization temperature of about 750 to 900° C. Hereinthe volume fraction between the crystalline high quartz mixed crystalphase and the glassy phase can be controlled in such a way that acoefficient of thermal expansion of about 0 is reached. To this endnormally a fraction of about 80 vol.-% high quartz mixed crystals toabout 20 vol.-% residual glass is desired. By controlling the fractionbetween the crystalline phase of high quartz mixed crystals and theresidual glass the characteristics may be adjusted within particularbounds.

However, the range of application of these glass ceramics is limited toabout 600° C., while already between 130° C. and 300° C. particularrestrictions exist.

In addition, it is known from U.S. Pat. No. 6,515,263, that glasses ofthe system Li₂O—Al₂O₃—SiO₂ may be transformed into glass ceramics (LASglass ceramics) having high quartz mixed crystals and/or keatite mixedcrystals as dominant crystals phases. If after nucleation in the rangebetween 600° C. and 800° C. a further temperature increase until about900 to 1200° C. is performed, then the previously formed high quartzmixed crystals further transform into keatite mixed crystals (U.S. Pat.No. 6,515,263). The transformation into keatite mixed crystals comestogether with a crystal growth, i.e. an increase in crystal size, thisleading to an increased light dispersion, i.e. light transmission isreduced at the same time. The glass ceramic article thereby has anincreasingly opaque appearance. According to U.S. Pat. No. 6,515,263 ashort-time temperature increase up to 1100° C. or more is performed,whereby the glass ceramic is transformed into a ceramic havingpredominantly a keatite mixed crystal phase in the core and having ahigh quartz mixed crystal phase close to the surface. These glassceramics have a coefficient of thermal expansion smaller than1.5×10⁻⁶/K.

However, formed bodies prepared from such a glass ceramic up to now aremerely utilized as components in series production. These formed bodiesare utilized in transparent or opaque state as cooking surfaces orcooking utensils or as fire-proof glass, as fireplace glasses, cookingutensils or as windows for pyrolysis hearths. In particular, for theapplication as cooking surfaces, a coefficient of thermal expansionsmaller than 1.5×10−6/K is necessary, and a coefficient of thermalexpansion of 0×10−6/K is, preferably, desired during manufacture.

In addition, for particular applications composite components aredesired which consist of a first component of a glass ceramic and of asecond component of a metal. For instance, the glass ceramic componentmay have the necessary precision, shape precision and temperaturestability, while the second component of metal is necessary to guaranteea precise mounting of the composite component and a stable connectiontechnique.

In the manufacture of composite components of a ceramic or glass ceramicand of a metal the major problem normally rests in the differencesbetween the coefficients of thermal expansion, since metals have atendency to a coefficient of thermal expansion that is considerablyhigher than that of ceramics or glass ceramics.

SUMMARY OF THE INVENTION

Thus, it is a first object of the invention to disclose a glass ceramicthat can easily be combined with a component made of a metal having alow coefficient of thermal expansion, such as Invar®.

It is a second object of the invention to disclose a glass ceramicoffering a high temperature stability in excess of 600° C.

It is a third object of the invention to disclose a glass ceramic thatis suitable for the manufacture of high-precision parts used for opticaland/or mechanical applications.

It is a forth object of the invention to disclose a glass ceramic thatis suitable for the manufacture of high-precision parts having superiorcharacteristics when prepared with known glass ceramics, in particularhaving a good form stability, temperature stability and/or irradiationstability.

It is a fifth object of the invention to disclose a high-precisioncomponent made of a glass ceramic and having superior characteristicswhen prepared with known glass ceramics, in particular having a goodform stability, temperature stability and/or irradiation stability.

It is a sixth object of the invention to disclose a method for themanufacture of such a glass ceramic or such a component.

It is a further object of the invention to disclose new applications ofa lithium-aluminosilicate glass ceramic.

These and other objects of the invention are solved according to theinvention by a component consisting of a lithium-aluminosilicate glassceramic wherein the crystalline fraction consists of at least 80 vol.-%,in particular of at least 85 vol.-%, preferably of at least 90 vol.-% ofkeatite mixed crystals, and wherein the coefficient of thermal expansionis between 1.5×10⁻⁶/K and 3×10⁻⁶/K.

The object of the invention is completely solved in this way.

A component made of such a keatite glass ceramic offers, particularlyadvantageous characteristics due to the fact that it practicallyconsists only of the stable keatite mixed crystal phase and that almostno high quartz residual phase is existent.

In particular such a component can be utilized at temperaturesconsiderably above 600° C., namely up to about 1000° C. or even higherfor short-time applications.

In addition, such a component offers a good irradiation resistance (i.e.for space applications). Also any hysteresis effect, such as known forinstance with respect to the glass ceramic Zerodur®, does not occur.

Due to the higher coefficient of thermal expansion which is in the rangeof about 1.5×10⁻⁶/K to 3×10⁻⁶/K, but normally in the range of about2.0×10⁻⁶/K, such components can, in addition, be combined particularlyadvantageously with components consisting of alloys having a lowcoefficient of thermal expansion, such as Invar®. In this regard thedifferences between the coefficient of thermal expansion may be kept to1×10⁻⁶/K, preferably to O.5×10⁻⁶/K, in particular to 0.1×10⁻⁶/K at themost, in the range between 0° C. and 250° C. Thereby, the connectiontechnique is considerably simplified in this temperature range.

Surprisingly it has been found that the desired range of the coefficientof thermal expansion can be reached, in particular when utilizing anaddition of 3 to 15 weight-% of P₂O₅ to the base glass. Fine adjustmentcan be made by the addition of P₂O₅ on the one hand or by the fractionof the keatite phase on the other hand.

In particular such components in which the crystalline fraction of thelithium-aluminosilicate glass ceramic is almost completely formed bykeatite mixed crystals, due the higher stability of the keatite mixedcrystal phase, new application fields are opened, i.e. applications asstages for micro-lithography applications, as mirrors, as spacers, ascalibrating bodies or as precision reflectors in resonators ofhigh-performance laser systems.

Since according to the invention keatite glass ceramic components areprepared by casting, also large components can easily be prepared, bycontrast to sintered components.

The sintered glass ceramic also offers a good long-term stability and ahigh resistance against chemical environmental influences.

Suitable components of keatite glass ceramic may be prepared by thefollowing steps:

-   -   casting a lithium-aluminosilicate base glass into a mold;        -   annealing for nucleation at a nucleation temperature of            about 600 to 900° C.;        -   annealing for the formation of a keatite glass ceramic at a            keatite formation temperature of about 800 to 1300° C.,            until the crystalline phase has been transformed almost            completely into keatite mixed crystals;    -   cooling the glass ceramic component to room temperature.

Herein basically it is possible, after annealing at nucleationtemperature, initially to anneal at a higher crystallisation temperaturefor crystallization, and to subsequently further increase thetemperature, to transform the initially formed high quartz mixedcrystals almost completely into keatite mixed crystals.

After casting of the base glass or after annealing for nucleation orcrystallization, the body thus formed can initially be inspected in itstransparent state for its inner quality (bubbles, inclusions,inhomogeneities, striae etc.), before the transformation into an opaquebody is performed by a further annealing.

Alternatively, also initially a glass ceramic that comprises high quartzmixed crystals as the major crystal phase can be prepared by initiallyannealing at nucleation temperature and by subsequent annealing atcrystallization temperature. Thus for instance from the base glass forthe manufacture of Zerodur® glass ceramic, initially Zerodur® glassceramic may be prepared which predominantly consists of the high quartzmixed crystal phase and that has a coefficient of thermal expansionclose to zero. By a subsequent heating and annealing to the higherkeatite formation temperature, the high quartz mixed crystals formedbefore can almost completely be transformed into keatite mixed crystals.

Alternatively, also it may be operated without any intermediate coolingsteps, or after annealing for nucleation at a lower temperature in theregion of about 650 to 850° C., immediately it can be heated to thehigher temperature necessary for keatite formation (in the region ofabout 800 to 1300° C.).

Also a three-step process cycle is possible by annealing initially atnucleation temperature in the region of about 650 to 850° C., with asubsequent annealing at crystallization temperature in the region ofabout 750 to 900° C. (for forming the high quartz crystal phase),followed by an annealing at keatite formation temperature in the regionbetween about 850 and 1300° C. for effecting transformation of the highquartz mixed crystals into keatite mixed crystals.

Annealing for keatite formation is preferably performed at least 900°C., preferably at least 1000° C., for at least one hour, in particularfor at least two hours, particularly preferred for a duration of aboutthree to four hours.

At a higher temperature the holding time may be shortenedcorrespondingly.

According to the method according to the invention annealing for keatiteformation is preferably performed at such a temperature and for such atime that the crystalline fraction is largely transformed into keatite.Preferably, herein at least 80 vol.-%, in particular about 85 vol.-%,and particularly preferred at least about 90 vol.-% of the crystallinefraction of the material are transformed into keatite mixed crystals.

Preferably, herein annealing is performed with a sufficient temperatureand for a sufficient time, until the high quartz mixed crystal phase,which is not sufficiently stable, has almost completely been transformedinto the stable keatite mixed crystal phase. At the most than a glassyresidual phase may exist which may be enriched with high quartz mixedcrystals and the insoluble ingredients, such as Na₂O and alkaline earthoxides, such as CaO, SrO, BaO. However, preferably any possible residualglassy phase exists only in the form of inclusions which are dispersedwithin a microstructure predominantly consisting of keatite mixedcrystals.

After completion of the heat treating the material usually comprises atleast 80 vol.-% or even 85 vol.-% of keatite (fraction of the totalvolume).

By such a structure high form stability and temperature stability in theregion of 550° C. to about 1000° C. is guaranteed. If a larger fractionof high quartz mixed crystal phase or glassy phase would be existent inthe overall body, then the form stability and temperature stability attemperatures above 600° C. or at even higher temperatures could possiblybe impaired.

According to a preferred development of the invention the glass ceramiccomponent, after casting of the base glass and/or after annealing, ismechanically finished, in particular ground, polished or lapped.

In this way the necessary forming, surface characteristics and formprecision can be reached by mechanical treatment (preferably with CNCcontrolled machines) by operations known in the art of glass processing.

As a base glass for the preparation of keatite glass ceramic componentspreferably a glass is utilized comprising the following components (inweight percent):

SiO₂: 50-75 Al₂O₃: 17-30 Li₂O: 2-8 B₂O₃: 0-5 P₂O₅:  0-15 SnO₂ + ZrO₂ +TiO₂: 0.1-7   Na₂O + K₂O + Cs₂O: 0-6 CaO + MgO + SrO + BaO + ZnO: 0-8refining agents such as Sb₂O₃, As₂O₃, 0-3 SnO₂, CeO₂, sulfate orchloride compounds: coloring oxides such as V₂O₅, Cr₂O₃, MnO,  0-5.Fe₂O₃, CoO, NiO and other oxides:

Herein preferably a base glass is utilized that comprises the followingcomponents (in weight percent):

SiO₂:   55-70% Al₂O₃:   19-25% Li₂O: 2.5-4.5 B₂O₃: 0-1 P₂O₅: 3-8 SnO₂ +ZrO₂ + TiO₂: 0.5-5   Na₂O + K₂O + Cs₂O: 0.1-3   CaO +MgO + SrO + BaO +ZnO: 0-5 refining agents such as Sb₂O₃, As₂O₃, 0-2 SnO₂, CeO₂, sulfateor chloride compounds: coloring oxides such as V₂O₅, Cr₂O₃, MnO,  0-2.Fe₂O₃, CoO, NiO and other oxides:

With such a lithium-aluminosilicate base glass the desired predominantformation of a keatite phase in the keatite glass ceramic component canbe obtained. Silicon oxide, aluminum oxide and lithium oxide are allnecessary in the given range to effect some crystallization and a lowthermal expansion. Preferably, boron oxide is not added at all or onlyin small amounts, since higher boron oxide contents are disadvantageousfor crystallization. As a further component P₂O₅ may be added, inamounts of 0 to 15 weight percent, preferably between 3 and 8 weightpercent, particularly, to allow a fine adjustment of the coefficient ofthermal expansion. Mandatory is the addition of ZrO₂ or TiO₂ asnucleation initiators. Alternatively, or in addition, also SnO₂ may beadded. The addition of the alkalis Na₂O, K₂O, Cs₂O as well as thealkaline earths CaO, SrO, BaO improves the meltability and thedeglassing characteristics of the glass during manufacture. MgO and ZnOact in a similar way. The glass ceramic may be prepared while addingcommon refining agents, such as e.g. As₂O₃, Sb₂O₃, SnO₂, CeO₂, sulfateor chloride compounds, such as NaCl. Also coloring oxides, such as V₂O₅,Cr₂O₃, MnO, Fe₂O₃, CoO, NiO and other oxides may be present in the givenranges.

Preferably, a composition may be utilized which corresponds to the knowncomposition of Zerodur® or Zerodur-M® sold by the applicant. Inaddition, also other similar glass ceramics may be utilized as a baseglass, such as Ceran®, Robax®, Clearceram®, Neoceram®, Astrositall®.

It will be understood that the above-mentioned and following features ofthe invention are not limited to the given combinations, but areapplicable in other combinations or taken alone without departing fromthe scope of the present invention.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

Further features and advantages of the invention will become apparentfrom the following description of a preferred embodiment.

According to the invention a component consisting of a special keatiteglass ceramic is disclosed that predominantly consists of keatite mixedcrystals.

Such a component is prepared from a base glass by casting and issubsequently transformed by heat treating into a keatite glass ceramicpredominantly consisting of a keatite mixed crystal phase.

The resulting coefficient thermal expansion of the keatite glass ceramicbetween 20° C. and 200° C. or even between 20° C. and 700° C. is in therange of about 1.5×10⁻⁶/K to 3×10⁻⁶/K, however, preferably is about2.0×10⁻⁶/K.

Highly stable components can be reached even at large dimensions. Thuseven diameters of eight meters at a thickness of 20 cm or more areachievable.

Glass ceramic components prepared according to the invention candirectly be utilized, e.g. as temperature stable or irradiationresistant precision components, such as for satellite applications, ormay be combined with metallic components consisting of alloys with a lowcoefficient of thermal expansion (such as Invar36® or the iron/nickelalloy 1.3912). In this regard a “low” coefficient of thermal expansionmay be regarded as a coefficient of thermal expansion that is smallerthan 3×10⁻⁶/K, in particular smaller than 2.5×10⁻⁶/K. The coefficient ofthermal expansion of Invar36® in the range between 20° C. and 90° C. isabout 1.7 to 2.0×10⁻⁶/K, whereby a particularly good matching with thekeatite glass ceramic according to the invention is reached.

Herein the combination with the metallic component may be reached by aclamping joint, by a screw connection, a positive fit connection, africtional fit, or possibly by a shrink fit or a glued joint.

EXAMPLE

A base glass consisting of the following components (in weight percent)was molten:

SiO₂ 55.5 Al₂O₃ 25.3 P₂O₅ 7.90 Li₂O 3.70 Na₂O 0.50 MgO 1.00 ZnO 1.40TiO₂ 2.30 ZrO₂ 1.90 As₂O₃ 0.50.

This corresponds to a possible composition of the glass ceramic sold bythe applicant under the trademark Zerodur®. The base glass manufacturedin this way after refining was cast into a blank glass block andthereafter ceramized by controlled crystallization, while utilizing atemperature program. To this end initially heating up to 730° C. wasperformed at 0.1 K/min, 730° C. were maintained for a duration of 24hours, subsequently heating up to 850° C. was performed at 0.1 K/min,this followed by a further holding at 850° C. for 48 hours, thisfollowed by a slow cooling to room temperature at 0.1 K/min.

Depending on the size of the glass ceramic block this temperatureprofile must be adjusted accordingly to yield a high precisioncrack-free glass ceramic having a high quartz mixed crystal phase in thedesired range.

From a glass ceramic block of predominant high quartz crystal phasemanufactured in this way, a suitable blank part was cut out,mechanically processed at its surface and inspected for its quality.

Thereafter, heating up to 1000° C. was performed, e.g. at 4 K/min,followed by a holding at this temperature for a time of four hours,before a controlled cooling to room temperature was performed at 4K/min.

The keatite glass ceramic component manufactured thereby was completelyopaque and consists mainly of the stable keatite mixed crystal phase.Also only a small glassy residual fraction is existent. The componentmanufactured thereby can be mechanically processed, e.g. sawed, ground,lapped or polished, to reach the necessary shape and surfacecharacteristics.

A component thus manufactured may, e.g., be combined by a positive fitconnection with a component of Invar36®, to thereby prepare a compositecomponent which may be utilized as a precision reflector in a resonatorof a high-performance laser system. Herein, also the good remissioncharacteristics are utilized apart from the good temperature stabilityof the material.

1. A composite component comprising at least a first component made of alithium-aluminosilicate glass ceramic comprising at least 70 vol.-%, ofkeatite mixed crystals, the coefficient of thermal expansion of thecomponent being between 1.5×10⁻⁶/K and 3×10⁻⁶/K in the temperature rangeof 20° C. to 700° C., and comprising (in wt.-%): SiO₂: 50-75 Al₂O₃:17-30 Li₂O: 2-8 B₂O_(3:) 0-5 P₂O_(5:)  0-15 SnO₂ + ZrO₂ + TiO₂: 0.1-7  Na₂O + K₂O + Cs₂O: 0-6 CaO + MgO + SrO + BaO + ZnO: 0-8 refining agents:0-3 coloring oxides and other oxides: 0-5

and further comprising at least a second component of an iron/nickelalloy having a coefficient of thermal expansion of 3×10⁻⁶/K at the mostbetween 0° C. and 200° C.
 2. The composite component of claim 1, whereinthe difference between the coefficients of thermal expansion of thefirst and second components between 0° C. and 200° C. is 1×10⁻⁶/K at themost.
 3. The composite component of claim 1, wherein the differencebetween the coefficients of thermal expansion of the first and secondcomponents between 0° C. and 200° C. is 0.5×10⁻⁶/K at the most.
 4. Thecomposite component of claim 1, wherein the difference between thecoefficients of thermal expansion of the first and second componentsbetween 0° C. and 200° C. is 0.1×10⁻⁶/K at the most.
 5. The compositecomponent of claim 1, wherein the first and second components areinterlocked by a connection selected from the group consisting of aclamping joint, a screw connection, a shrink joint, a positive fitconnection and a glued joint.